1-Naphthalenealanine

Modify Date: 2025-08-25 16:52:44

1-Naphthalenealanine Structure
1-Naphthalenealanine structure
Common Name 1-Naphthalenealanine
CAS Number 28095-56-9 Molecular Weight 215.248
Density 1.3±0.1 g/cm3 Boiling Point 412.3±33.0 °C at 760 mmHg
Molecular Formula C13H13NO2 Melting Point 239℃
MSDS Chinese USA Flash Point 203.2±25.4 °C

 Use of 1-Naphthalenealanine


2-Amino-3-(naphthalen-1-yl)propanoic acid is an alanine derivative[1].

 Names

Name h-dl-1-nal-oh
Synonym More Synonyms

 1-Naphthalenealanine Biological Activity

Description 2-Amino-3-(naphthalen-1-yl)propanoic acid is an alanine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1077.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 412.3±33.0 °C at 760 mmHg
Melting Point 239℃
Molecular Formula C13H13NO2
Molecular Weight 215.248
Flash Point 203.2±25.4 °C
Exact Mass 215.094635
PSA 63.32000
LogP 2.34
Vapour Pressure 0.0±1.0 mmHg at 25°C
Index of Refraction 1.660
Storage condition 2-8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922499990

 Synthetic Route

 Customs

HS Code 2922499990
Summary HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

 Articles21

More Articles
Synthesis and characterization of more potent analogues of hirudin fragment 1-47 containing non-natural amino acids.

Biochemistry 37(39) , 13507-15, (1998)

Hirudin is the most potent and specific inhibitor of thrombin, a key enzyme in the coagulation process existing in equilibrium between its procoagulant (fast) and anticoagulant (slow) form. In a previ...

The A14 position of insulin tolerates considerable structural alterations with modest effects on the biological behavior of the hormone.

J. Protein Chem. 11(5) , 571-7, (1992)

As part of our aim to investigate the contribution of the tyrosine residue found in the 14 position of the A-chain to the biological activity of insulin, we have synthesized six insulin analogues in w...

Adding L-3-(2-Naphthyl)alanine to the genetic code of E. coli.

J. Am. Chem. Soc. 124 , 1836-1837, (2002)

An unnatural amino acid, L-3-(2-naphthyl)alanine, has been site-specifically incorporated into proteins in Escherichia coli. An orthogonal aminoacyl-tRNA synthetase was evolved that uniquely aminoacyl...

 Synonyms

L66J B1YZVQ
2-amino-3-naphthalen-1-ylpropanoic acid
1-naphthalanine
3-(1-Naphthyl)-DL-alanine
3-(1-Naphthyl)alanine
D,L-β-(1-Naphthyl)alanine
1-Naphthalenealanine
D,L-1-naphthylalanine
2-Amino-3-(1-naphthyl)propanoic acid
1-Naphthalenepropanoic acid, α-amino-
2-amino-3-(naphthalen-1-yl)propanoic acid (non-preferred name)
MFCD00067507
2-Amino-3-(1-naphthalenyl)propanoic acid
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